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Research Advances on the Pathogenesis and Treatment of Hemolytic Uremic Syndrome --Review / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 636-640, 2022.
Article in Chinese | WPRIM | ID: wpr-928767
ABSTRACT
Hemolytic uremic syndrome (HUS) is clinically rare, with high mortality and case fatality rates. In recent years, the research on HUS has been intensified and the pathophysiological mechanism has been continuously improved. At present, the main mechanism of pathogenesis is the excessive activation of complement alternative pathways mediated by complement-related gene mutations or the existence of antibodies. The treatment methods and strategies are also constantly updated, mainly including complement-blocking drugs such as Eculizumab, Lavalizumab, and Ravulizumab. In this review, the new developments in the pathogenesis and treatment of HUS is summarized, and provide references for the clinical treatment of HUS.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Complement System Proteins / Hemolytic-Uremic Syndrome / Mutation Type of study: Etiology study Limits: Humans Language: Chinese Journal: Journal of Experimental Hematology Year: 2022 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Complement System Proteins / Hemolytic-Uremic Syndrome / Mutation Type of study: Etiology study Limits: Humans Language: Chinese Journal: Journal of Experimental Hematology Year: 2022 Type: Article